The present disclosure relates generally to medical devices. More specifically, the disclosure relates to devices and methods for occluding or closing a body vessel using a radiofrequency signal to transmit energy, heat, and/or ablate the body vessel.
There are numerous medical conditions when it is desired or necessary to close a body vessel, including the treatment of aneurysms, arteriovenous malformations, arteriovenous fistulas, for starving organs of oxygen and nutrients, in the treatment or containment of cancerous growths, and so on.
Several techniques are known and in use for closing or occluding such body vessels. Traditionally, vessels have been closed by means of external ligation, which generally must be carried out by an open surgery procedure, with its associated risks, inconvenience, and long patient recovery times. Other, more recent, methods aim to use an endoluminal procedure to insert into the vessel or organ one or more occlusion devices, such as a metal framed occluder, coils, pellets or the like, able to obstruct the flow of blood in the vessel.
It is also known to constrict a vessel by endoluminal ablation, causing contraction of the vessel and/or coagulation of blood to form a blood clot in the vessel. Various methods can be employed to cause such ablation.
The invention may include any of the following embodiments in various combinations and may also include any other aspect described below in the written description or in the attached drawings. This disclosure provides a medical device and methods for conducting vessel ablation and occlusion.
The medical device(s) of this disclosure transmits energy to the body vessel to cause vessel ablation. The energy source can be a radiofrequency (“RF”) signal generated by a power supply and/or signal generator. The device includes an elongate member including a first conductive element (e.g. first electrode in AC system or anode in DC system) and a basket. The elongate member has a proximal end and extends to a distal end, defining a longitudinal axis A. The elongate member includes the first conducive element.
In one aspect, the basket includes a hub (e.g. first hub) and a circumferential body, the hub disposed about the elongate member. The circumferential body extends radially and distally from the hub to an open end, in an expanded state. The circumferential body has a surface (e.g. inner or outer surface) such that a membrane is disposed on the surface and is substantially impermeable or impeding to blood flow such that the membrane occludes the blood flow in the expanded state.
The device further includes a second conductive element (e.g. second electrode in AC system or cathode in DC system) being one of the basket and a return electrode disposed outside of the body vessel when the circumferential body and device is in the expanded state.
In a second aspect, the basket includes a pair of hubs (e.g. proximal and distal hubs) and a cylindrical portion. The basket is disposed about the elongate member. The cylindrical portion is disposed between the proximal and distal hubs. The cylindrical portion has a first end attached to the proximal hub and distally extends to a second end attached to the distal hub. The cylindrical portion is radially expanded in an expanded state. The cylindrical portion also includes a plurality of struts being interlocked or braided together and having an interlocked or braided structure being substantially impermeable or impeding to the blood flow such that the interlocked structure occludes the blood flow in the expanded state.
In any aspect, the basket (e.g. circumferential body or cylindrical portion) is movable between a collapsed state for delivery and the expanded state for treatment in the vessel. The device further includes a second conductive element being one of the basket, in either aspect, and a return electrode disposed outside of the body vessel in the expanded state.
In any aspect, the device further includes a control unit being operatively coupled to the first conductive element. In the first aspect, the control unit and the first and second conductive elements form a first electrical circuit such that the control unit actuates the device to transmit energy to the body vessel. In the second aspect, the control unit and the first and second conductive elements form a second electrical circuit such that the control unit actuates the device to transmit energy to the body vessel.
In any aspect, the device can be part of an assembly including an outer sheath. The outer sheath has a first sheath end and extending to a second sheath end and forming a lumen therethrough. The elongate member is slidably received within the lumen, having any of the features described herein. The basket in any aspect discussed herein may be disposed about the elongate member in the assembly.
Various additional features and embodiments will become apparent with the following description. The present disclosure may be better understood by referencing the accompanying figures.
The present disclosure will now be described more fully with reference to the accompanying figures, which show various embodiments. The accompanying figures are provided for general understanding of various embodiments and method steps. However, this disclosure may be embodied in many different forms. These figures should not be construed as limiting, and they are not necessarily to scale.
The following definitions will be used in this application.
“About” or “substantially” mean that a given quantity (e.g. lengths or volumes) is within 10%, preferably within 5%, more preferably within 1% of a stated value. For example, a first quantity of length can be within 10% of a second length quantity. “Substantially impermeable” means that a structure (e.g. basket) blocks essentially all blood flow, while it may have some small pores or holes that allow some substances to pass through and/or a negligable amount of blood flow.
“Adjacent” referred to herein is near, near to, or in close proximity with.
“Longitudinally” and derivatives thereof will be understood to mean along the longitudinal axis of the device.
The terms “proximal” and “distal” and derivatives thereof will be understood in the frame of reference of a physician using the device. Thus, proximal refers to locations closer to the physician and distal refers to the locations farther away from the physician (e.g., deeper in the patient's vasculature).
“Radially” and derivatives thereof will be understood to mean along a radial axis of the body vessel. Likewise, “radial force” and derivatives thereof will be understood to mean a force applied along the radial axis.
The present disclosure discusses a device 10 to perform vessel ablation by transmitting energy to a body vessel having a blood flow. The target vessels for the present disclosure may be any vessel. For example, the target vessels may be small arteries (possibly down to 1 millimeter in diameter) that require a device with a low profile. Generally, the device will have two conductive elements operable to create an electric field. In one example, applying a radiofrequency signal generates the field, and the field heats the local environment in the body vessel (including the blood flow and the vessel wall) to cause swelling and occluding of the body vessel at a target site.
Generally using radiofrequency (“RF”) signal, electrical terminal(s)/conductive element(s) are fed endoluminally into the vessel and an electrical pulse and/or constant electrical signal at RF frequencies is applied to the conductive element(s). The conductivity of blood and/or the vessel tissues causes localized heating of the blood and tissue and not significant heating of the conductive elements themselves, creating a local zone or environment that is heated by the RF frequencies. This heating can be used to cause damage to the tissue (intima) of the vessel wall, resulting in vessel contraction. Additionally or alternatively, RF ablation heats the surrounding blood, causing the blood and vessel wall to coagulate around the electrical terminal and form a blood clot and/or embolization which blocks the vessel.
Two types of RF ablation systems are generally contemplated in the art: a monopolar system and a bipolar system. A monopolar system may have an elongate first electrode (e.g. active electrode) and a second electrode (e.g. dispersive electrode) pad or return electrode positioned outside the patient's body. The first electrode is designed to be fed endoluminally into the patient's vessel, while the second electrode pad is positioned against the person's outer body, as close as practicable to the first electrode. In a bipolar system, both electrodes are present in one device and inserted endoluminally into the vessel. Electrical energy applied to the first electrode will pass by conduction to the second electrode. There can be localized heating at the electrodes, which effects the desired ablation.
Advantageously, operating the device having a monopolar system may be easier for manufacturing and use with multiple and/or different return electrode configurations. Alternatively advantageously, operating the device having a bipolar system may be easier for the user by not having a separable return electrode disposable outside of the body.
The RF frequencies, and the power they generate, may not be large enough to heat the first electrode and/or the second or return electrode. However, the RF signal and field generated will cause localized heating of the surrounding blood and tissue. The temperature of the electrodes will likely elevate over body temperature; however, heat is primarily generated in the surrounding tissue.
In one aspect, the RF energy could be an AC signal from about 100 kHz to about 1 MHz. More specifically, the AC signal could be about 400 to about 500 kHz. The signal may also be a DC signal. The signal may vary over time, and can depend on the required power to maintain a desired temperature in the body vessel.
Power=Current×Voltage Voltage=Current×Resistivity
Power=Current2×Resistivity=Voltage2/Resistivity
Generally, the device 10 (as depicted in both
Controlling or preventing local blood flow can also have an advantage of allowing a practitioner using a device of this disclosure to use lower energy and perform faster embolization and ablation than with devices that do not prevent or reduce local blood flow.
In some cases, the basket itself is a second conductive element for the device (e.g. bipolar system). In general, baskets such as those depicted in this disclosure can provide the advantage of creating a larger electrical field for larger body vessels. Their larger size and surface area can spread out the electrical field. Additionally, these baskets can focus the electrical field between the first and second conductive elements, and assist in centering the first conductive element in the vessel. These, and further, advantages will be discussed in detail below.
In
Also as discussed above, the device includes a second conductive element 36 being one of the basket 38 and a return electrode (
The device 10 also includes a control unit (
The device may optionally further include an outer sheath 32 having a first sheath end (
The outer sheath 32 forms a lumen 79 therethrough such that the elongate member 24 is slidably disposed in the lumen 79. If the second conductive element 36 is the basket 38, the control unit and the first and second conductive elements form the first electrical circuit. In this case, the second conductive element 36 is circumferentially disposed about the longitudinal axis and the elongate member 24.
Alternatively, if the second conductive element 36 is the return electrode, the control unit, the first conductive element, and the return electrode form another type of electrical circuit having a modified path. Additionally or alternatively, the elongate member 24 may form a loop or curved hook at its respective distal end so that it comes into closer contact with the vessel wall during use. As the vessel wall swells, the curved distal end may come into contact with the vessel wall and facilitate ablation and/or heating. For example, the first elongate member 24 can have a loop or hook at the distal end 28.
The device 10 can further include an isolator 48 disposed about the first conductive element 34 to electrically isolate and/or insulate the first conductive element 34 from the rest of the device. The isolator 48 could be a shrink tubing heat shrunk and/or immobilized about or onto the first elongate member 24. The isolator 48 may have a first isolator end distal the proximal end 26. The isolator may extend to a second isolator end proximal the distal end 28, creating exposed ends of the elongate member. In this way, even if the first conductive element 34 extends from the proximal end 26 and to the distal end 28, it will have a central region electrically isolated from the second conductive element 36 and the rest of the device.
The first hub 80 may be fixedly attached to the isolator 48 such that the first hub 80 and the elongate member do not move relative to each other. However, the first hub 80 could also be slidably disposed about the isolator 48, including the isolator 48 having a lubricious coating to accommodate easy sliding between components.
Additionally, the device 10 can include a temperature sensor 30 (thermistor, thermocouple, and the like) integrated into the device at a suitable location. In
In a third aspect, the temperature sensor could be integrated at one end (e.g. 78) of an outer sheath 32 (e.g. active or passive microcatheter). In a fourth aspect, the temperature sensor could be a separate device mounted at the tip of a delivery wire, allowing completely independent positioning of the temperature sensor relative to the conductive elements and other parts of the device.
In any case, sufficient electrical shielding may be needed between components of the device 10 conducting RF energy and the temperature sensor because it can be difficult to sense temperature and conduct energy/electricity reliably if these components are too close to each other. One way of overcoming this interference is to alternate between ablation and temperature measurement so that ablation is performed out-of-phase with the temperature measurement. In one aspect, the practitioner may ablate for 900 milliseconds, and then measured temperature for 100 milliseconds, continuously repeating this 1 second pattern. Other time increments are also contemplated.
Another possible solution to the possible interference between temperature sensing and conducting energy is by electrical filtering of the temperature signal. Some examples include using RF chokes to block higher-frequency AC and/or low-pass filtering where the high-frequency interference is attenuated and the lower-frequency temperature signal is admitted.
It is also contemplated to use a first material for the temperature sensor 30 and a different, second material for the conductive elements (34, 36) to further avoid any interference. In one example, the temperature sensor and/or thermistor could be made of Nifethal® (a nickel/iron alloy), available from Kanthal, Hallstahmmar, Sweden. Temperature could be measured by the change in resistance of the material used.
In one example, the second connector 44 is connected to the control unit 58 and extends to the basket 38. The elongate member 24 can be directly connected to the control unit 58 or connected to the control unit 58 by way of the first connector 40. In one example, the control unit 58, the elongate member 24, the basket 38, and the second connector 44 form the first electrical circuit. The first connector 40 may also be included in the first electrical circuit.
While
The first hub 80 includes a tubular segment disposed about the elongate member 24. The circumferential body 81 includes a plurality of ribs or struts (e.g. 63) wherein each strut 63 has a first strut end connected to the first hub 80 and extends radially and distally from the tubular segment to the open end 77 in the expanded state. The plurality of struts could have the overall geometry of a spherical cap, polygon, ellipsoid, and the like when the basket is in the expanded state.
While
Nitinol is a metal alloy of nickel and titanium having a unique shape memory setting property and being biocompatible. At a transition temperature, Nitinol may undergo a phase change from Martensitic to Austenite, changing its structure. Here, the basket could be heat set or pre-set to the expanded state and maintained in the collapsed or delivery state (shown in
Turning to a second aspect,
The proximal hub 84 and the cylindrical portion 82 have one or more struts (e.g. 65) being braided or interlocked together and forming an interlocked or braided structure 64. The interlocked structure 64 is substantially impermeable to the blood flow such that it occludes the blood flow in the expanded state, having the advantages discussed herein. In some examples, the interlocked structure 64 can block or occlude greater than about 50% of the blood flow to about 100% of the blood flow by covering the cross-sectional area of the vessel. In this way, the interlocked structure 64 can impede or be substantially impermeable to the blood flow. Additionally or alternatively, a membrane similar to membrane 62 can be disposed about the surface (e.g. inner or outer) of basket 39 to occlude or assist in occluding blocking of blood flow.
The device of
The basket 39 can be formed by any manner known in the art to form a tight weave that blocks or impedes blood flow. For example, the basket 39 can be formed of a plurality of struts being interlocked, woven, knotted, braided, stamped, or cut to form the interlocked structure 64. The interlocked structure 64 can extend or be formed on the entire outer surface of the basket 39.
The features of the outer sheath 32, isolator 48, first and second conductive elements (34, 36), and various circuits discussed above with the first aspect can also apply to this second aspect. For example, the hubs (84, 86) could be fixed or slidable over the isolator 48. Also similar to the first aspect, the second aspect disclosed in
Likewise,
It will be appreciated that either basket 38 or 39 could facilitate centering the elongate member 24 and the first conductive element 34 in the body vessel and device. This may have the advantage of creating an electrical field that extends through largest volume possible in the vessel, and this may allow a focused electrical field between the first and second conductive elements.
In step 104, the occlusion 22 has fully formed and the vessel is closed. In step 105, the user or practitioner withdraws the device, leaving the occlusion 22 intact.
Similarly in
In step 108, the practitioner operates the device such that the RF signal and field start to form blood coagulation 14 and occlusion 22. The user may slowly withdraw the device as the occlusion forms. In step 109, the occlusion 22 is fully formed distal the basket. In step 110, the practitioner withdraws the device, leaving the occlusion 22 intact. Through these aspects, the inventors demonstrate various devices and methods to perform vessel ablation with an energy source.
Feature Combinations
The following feature combinations assist in understanding this disclosure. The device includes an elongate member including a first conductive element and a basket. The elongate member has a proximal end and extends to a distal end, defining a longitudinal axis A. The elongate member includes the first conducive element. The basket includes a proximal hub and a circumferential body, the proximal hub disposed about the elongate member. The circumferential body extends radially and distally from the proximal hub to an open end, in an expanded state. The circumferential body has a surface such that a membrane is disposed on the surface and is substantially impermeable to blood flow such that the membrane occludes the blood flow in the expanded state. The device further includes a second conductive element being one of the basket and a return electrode disposed outside of the body vessel in the expanded state.
The device includes a control unit being operatively coupled to the first conductive element. In the first aspect, the control unit and the first and second conductive elements form a first electrical circuit such that the control unit actuates the device to transmit energy to the body vessel.
Additionally or alternatively to the above combination(s), the device can optionally be part of an assembly including an outer sheath. The outer sheath has a first sheath end and extending to a second sheath end and forming a lumen therethrough. The elongate member is slidably received within the lumen. The basket may be disposed about the elongate member in the assembly.
Additionally or alternatively to the above combination(s), the distal end can optionally include the first conductive element, and the second conductive element is the basket such that the control unit, the first conductive element, and the second conductive element form the first electrical circuit.
Additionally or alternatively to the above combination(s), the second conductive element is optionally circumferentially disposed about the longitudinal axis.
Additionally or alternatively to the above combination(s), the device can optionally include a first connector connected to the control unit and extending to the basket, the elongate member being connected to the control unit such that the control unit, the elongate member, the basket, and the first connector form the first electrical circuit.
Additionally or alternatively to the above combination(s), the proximal hub can optionally include a tubular segment disposed about the elongate member, and the circumferential body comprises a plurality of ribs, each rib having a first end connected to the tubular segment, each rib extending radially and distally from the hub to the open end in the expanded state.
Additionally or alternatively to the above combination(s), the plurality of ribs can optionally form a spherical cap in the expanded state.
Additionally or alternatively to the above combination(s), the membrane can optionally be formed as a coating, which can be disposed on the entire surface of the basket.
Additionally or alternatively to the above combination(s), the device may optionally include an isolator disposed about the first conductive element to electrically isolate the first conductive element.
Additionally or alternatively to the above combination(s), the device may optionally include a temperature sensor.
Additionally or alternatively to the above combination(s), the second conductive element is the return electrode.
In a second aspect, the device has an elongate member including a first conductive element and a basket. The elongate member has a proximal end and extends to a distal end, defining a longitudinal axis A. The elongate member includes the first conducive element. The basket includes a pair of hubs and a cylindrical portion disposed therebetween. The cylindrical portion has a first end attached to the proximal hub and distally extends to a second end attached to the distal hub. The cylindrical portion is radially expanded in an expanded state, and the cylindrical portion includes a plurality of struts being interlocked together and forming an interlocked structure or braided structure being substantially impermeable or impeding to the blood flow such that the interlocked structure occludes the blood flow in the expanded state. The device further includes a second conductive element being one of the basket and a return electrode disposed outside of the body vessel in the expanded state.
The device includes a control unit being operatively coupled to the first conductive element. In the first aspect, the control unit and the first and second conductive elements form a second electrical circuit such that the control unit actuates the device to transmit energy to the body vessel.
Additionally or alternatively to the above combination(s), the device can optionally be part of an assembly including an outer sheath. The outer sheath has a first sheath end and extending to a second sheath end and forming a lumen therethrough. The elongate member is slidably received within the lumen. The basket may be disposed about the elongate member in the assembly.
Additionally or alternatively to the above combination(s), the distal end can optionally include the first conductive element, and the second conductive element is the basket such that the control unit, the first conductive element, and the second conductive element form the second electrical circuit.
Additionally or alternatively to the above combination(s), the second conductive element is optionally circumferentially disposed about the longitudinal axis.
Additionally or alternatively to the above combination(s), the device can optionally include a first connector connected to the control unit and extending to the basket, the elongate member being connected to the control unit such that the control unit, the elongate member, the basket, and the first connector form the second electrical circuit.
Additionally or alternatively to the above combination(s), the device may optionally include an isolator disposed about the first conductive element to electrically isolate the first conductive element.
Additionally or alternatively to the above combination(s), the device may optionally include a temperature sensor.
Additionally or alternatively to the above combination(s), the second conductive element is the return electrode.
Additionally or alternatively to the above combination(s), the device may optionally include a balloon disposed inside the basket, the balloon being inflatable to move the basket from a collapsed state to the expanded state.
It should be understood that the foregoing relates to exemplary embodiments of the disclosure and that modifications may be made without departing from the spirit and scope of the disclosure as set forth in the following claims. While the disclosure has been described with respect to certain embodiments it will be appreciated that modifications and changes may be made by those skilled in the art without departing from the spirit of the disclosure.
Number | Date | Country | |
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62322861 | Apr 2016 | US |